1185842-25-4

Basic information

• Product Name: N-[(4-Methoxylphenyl)(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide
• Synonyms: N-[(4-Methoxylphenyl)(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide
• CAS NO: 1185842-25-4
• Molecular Weight: 305.182
• Mol File: 1185842-25-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-[(4-Methoxylphenyl)(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(4-Methoxylphenyl)(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide(1185842-25-4)
• EPA Substance Registry System: N-[(4-Methoxylphenyl)(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]acetamide(1185842-25-4)

Safety Data

• Hazardous Substances Data: 1185842-25-4(Hazardous Substances Data)

Upstream product

• 171364-79-7 2-(4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 108-24-7 acetic anhydride 

Downstream Products

• 5267-47-0 N-((4-methoxyphenyl)(phenyl)methyl)acetamide 
• 1351866-43-7 (R)-(+)-N-[(4-methoxyphenyl)(4-methylphenyl)methyl]acetamide 
• 1351866-49-3 (S)-(+)-N-[(4-methoxyphenyl)(4-methylphenyl)methyl]acetamide 

Relevant articles and documents

Inversion or retention? Effects of acidic additives on the stereochemical course in enantiospecific suzuki-miyaura coupling of α-(acetylamino) benzylboronic esters

The stereochemical course of the stereospecific Suzuki-Miyaura coupling of enantioenriched α-(acetylamino)benzylboronic esters with aryl bromides can be switched by the choice of acidic additives in the presence of a Pd/XPhos catalyst system. Highly enant